Morpholine → 4-(4-Bromo-1,3-thiazol-2-yl)morpholine

HRID 40311

反応式

HRID 40311 の反応式
C(N(CC)C(C)C)(C)C.Br[C:11]1[S:12][CH:13]=[C:14]([Br:16])[N:15]=1.[NH:17]1[CH2:22][CH2:21][O:20][CH2:19][CH2:18]1>CCO>[Br:16][C:14]1[N:15]=[C:11]([N:17]2[CH2:22][CH2:21][O:20][CH2:19][CH2:18]2)[S:12][CH:13]=1

参加物

5

反応物 3

HCID 8083MorpholineHCID 81531DiisopropylethylamineHCID 27632972,4-Dibromo-1,3-thiazole

生成物 1

HCID 438110424-(4-Bromo-1,3-thiazol-2-yl)morpholine収率 68.5%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
140 °C

実験手順

To a microwave vial was added N,N-diisopropylethylamine (0.86 ml, 4.9 mmol), 2,4-dibromothiazole (1.00 g, 4.1 mmol), and morpholine (0.43 ml, 4.9 mmol) in EtOH (4 mL). The mixture was heated under microwave irradiation at 140° C. for 35 minutes. The reaction mixture was concentrated in vacuo. The crude material was dissolved in minimal DCM/MeOH and purified via MPLC (eluting with 0-30% EtOAc in hexanes) to yield 4-(4-bromothiazol-2-yl)morpholine (0.700 g, 68% yield) as a white solid.

後処理

  1. concentrationThe reaction mixture was concentrated in vacuo
  2. dissolutionThe crude material was dissolved in minimal DCM/MeOH
  3. custompurified via MPLC (eluting with 0-30% EtOAc in hexanes)

出典と根拠

ORDレコード
ord-f5d6627eee1f4de1a5d7c92be3874165
出典データセット
uspto-grants-2013_09
特許番号
US08524900B2

関連ノート

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